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      Significant polar vasculosis in a patient with a 30-year history of type 2 diabetes

      research-article
      1 , 1 , 1 , 1 , 1 , 1 , 2 , 1 , 3 , 4 , 3 , 1 , 2
      Endocrinology, Diabetes & Metabolism Case Reports
      Bioscientifica Ltd
      Adult, Male, Asian - Japanese, Japan, Kidney, Diabetes, Insulin, Diabetes mellitus type 2, Diabetic foot syndrome, Diabetic nephropathy, Diabetes mellitus type 2, Diabetic neuropathy, Diabetic nephropathy, Diabetic foot neuropathy, Retinopathy, Hypertension, Polar vasculosis*, Proteinuria, Peripheral oedema , Diabetic foot ulceration, Leg pain, Paraesthesia, Neovascularization*, Histopathology, Estimated glomerular filtration rate, Urinalysis, Haemoglobin A1c, Renal biopsy, Angiography, C-peptide (blood), Glucose (blood), Immunoglobulin A, Insulin, Creatinine (serum), Diet, Clopidogrel, Lansoprazole*, Nifedipine, Rosuvastatin*, Aspirin, Metformin, Insulin glulisine, Insulin degludec*, Nephrology, Unique/unexpected symptoms or presentations of a disease, November, 2019

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          Abstract

          Summary

          We report the renal histology of a 66-year-old man with hypertension, cardiovascular disease, and a 30-year history of type 2 diabetes mellitus with proliferative diabetic retinopathy, diabetic neuropathy, and diabetic foot status post toe amputation. Urinary protein excretion was 1.4 g/gCr, serum creatinine level 0.86 mg/dL, estimated glomerular filtration rate 69 mL/min/1.73 m 2, and HbA1c 13–15%, despite using insulin. Light microscopy showed global glomerulosclerosis in 37% of the glomeruli, but the remaining glomeruli were intact. Significant polar vasculosis was present, while arteriolar sclerosis was mild. Electron microscopy revealed a thickened glomerular basement membrane, which is compatible with the early stage of diabetic glomerulopathy. The presented case was unique because glomerular changes seen typically in diabetes were not seen in the patient, despite the long-standing history of diabetes and diabetic comorbidities, while prominent polar vasculosis was found. Polar vascular formation helps preserve the glomeruli by allowing hyperosmotic blood bypass the glomeruli; this decreases intraglomerular pressure and minimizes glomerular endothelial damage.

          Learning points:
          • A 66-year-old man with a 30-year history of type 2 diabetes mellitus with poor glycemic control underwent renal biopsy, which showed scarce glomerular changes typically seen in diabetic kidney disease and instead revealed significant polar vasculosis.

          • Past studies demonstrated that the increased small vessels around the vascular hilus in diabetic patients originated from the afferent arterioles and drained into the peritubular capillaries.

          • Polar vascular formation may preserve glomerular function by allowing the blood flow to bypass the glomeruli and decreasing the intraglomerular pressure, which minimizes endothelial damage of the glomerular tufts.

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          Most cited references14

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          Pathologic classification of diabetic nephropathy.

          Although pathologic classifications exist for several renal diseases, including IgA nephropathy, focal segmental glomerulosclerosis, and lupus nephritis, a uniform classification for diabetic nephropathy is lacking. Our aim, commissioned by the Research Committee of the Renal Pathology Society, was to develop a consensus classification combining type1 and type 2 diabetic nephropathies. Such a classification should discriminate lesions by various degrees of severity that would be easy to use internationally in clinical practice. We divide diabetic nephropathy into four hierarchical glomerular lesions with a separate evaluation for degrees of interstitial and vascular involvement. Biopsies diagnosed as diabetic nephropathy are classified as follows: Class I, glomerular basement membrane thickening: isolated glomerular basement membrane thickening and only mild, nonspecific changes by light microscopy that do not meet the criteria of classes II through IV. Class II, mesangial expansion, mild (IIa) or severe (IIb): glomeruli classified as mild or severe mesangial expansion but without nodular sclerosis (Kimmelstiel-Wilson lesions) or global glomerulosclerosis in more than 50% of glomeruli. Class III, nodular sclerosis (Kimmelstiel-Wilson lesions): at least one glomerulus with nodular increase in mesangial matrix (Kimmelstiel-Wilson) without changes described in class IV. Class IV, advanced diabetic glomerulosclerosis: more than 50% global glomerulosclerosis with other clinical or pathologic evidence that sclerosis is attributable to diabetic nephropathy. A good interobserver reproducibility for the four classes of DN was shown (intraclass correlation coefficient = 0.84) in a test of this classification.
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            Renal Structure in Normoalbuminuric and Albuminuric Patients With Type 2 Diabetes and Impaired Renal Function

            OBJECTIVE The structural basis of normoalbuminuric renal insufficiency in patients with type 2 diabetes remains to be elucidated. We compared renal biopsy findings in patients with type 2 diabetes and estimated glomerular filtration rate (eGFR) and measured GFR of <60 mL/min/1.73 m2, associated with either normo-, micro-, or macroalbuminuria. RESEARCH DESIGN AND METHODS In patients with normo- (n = 8) or microalbuminuria (n = 6), renal biopsies were performed according to a research protocol. In patients with macroalbuminuria (n = 17), biopsies were performed according to clinical indication. Findings were categorized according to the Fioretto classification: category 1 (C1), normal/near normal; category 2 (C2), typical diabetic nephropathy (DN) with predominantly glomerular changes; and category 3 (C3), atypical with disproportionately severe interstitial/tubular/vascular damage and with no/mild diabetic glomerular changes. RESULTS In our study population (mean eGFR 35 mL/min/1.73 m2), typical glomerular changes (C2) of DN were observed in 22 of 23 subjects with micro- or macroalbuminuria compared with 3 of 8 subjects with normoalbuminuria (P = 0.002). By contrast, predominantly interstitial or vascular changes (C3) were seen in only 1 of 23 subjects with micro- or macroalbuminuria compared with 3 of 8 normoalbuminuric subjects (P = 0.08). Mesangial area increased progressively from normal controls to patients with type 2 diabetes and normo-, micro-, and macroalbuminuria. Varying degrees of arteriosclerosis, although not necessarily the predominant pattern, were seen in seven of eight subjects with normoalbuminuria. CONCLUSIONS Typical renal structural changes of DN were observed in patients with type 2 diabetes and elevated albuminuria. By contrast, in normoalbuminuric renal insufficiency, these changes were seen less frequently, likely reflecting greater contributions from aging, hypertension, and arteriosclerosis.
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              Patterns of renal injury in NIDDM patients with microalbuminuria.

              Microalbuminuria predicts overt nephropathy in non-insulin-dependent diabetic (NIDDM) patients; however, the structural basis for this functional abnormality is unknown. In this study we evaluated renal structure and function in a cohort of 34 unselected microalbuminuric NIDDM patients (26 male/8 female, age: 58 +/- 7 years, known diabetes duration: 11 +/- 6 years, HbA1c: 8.5 +/- 1.6%). Systemic hypertension was present in all but 3. Glomerular filtration rate (GFR) was 101 +/- 27 ml.min-1.1.73 m-2 and albumin excretion rate (AER) 44 (20-199) micrograms/ min. Light microscopic slides were categorized as: C I) normal or near normal renal structure; C II) changes "typical" of diabetic nephropathology in insulin-dependent diabetes (IDDM) (glomerular, tubulo-interstitial and arteriolar changes occurring in parallel); C III) "atypical" patterns of injury, with absent or only mild diabetic glomerular changes associated with disproportionately severe renal structural changes including: important tubulo-interstitial with or without arteriolar hyalinosis with or without global glomerular sclerosis. Ten patients (29.4%) were classified as C I, 10 as C II (29.4%) and 14 as C III (41.2%); none of these patients had any definable non-diabetic renal disease. GFR, AER and blood pressure were similar in the three groups, while HbA1c was higher in C II and C III than in C I patients. Diabetic retinopathy was present in all C II patients (background in 50% and proliferative in 50%). None of the patients in C I and C III had proliferative retinopathy, while background retinopathy was observed in 50% of C I and 57% of C III patients. In summary, microalbuminuric NIDDM patients are structurally heterogeneous with less than one third having "typical" diabetic nephropathology. The presence of both "typical" and "atypical" patterns of renal pathology was associated with worse metabolic control, suggesting that hyperglycaemia may cause different patterns of renal injury in older NIDDM compared to younger IDDM patients.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                EDM
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                12 November 2019
                2019
                : 2019
                : 19-0092
                Affiliations
                [1 ]Nephrology Center , Toranomon Hospital, Tokyo, Japan
                [2 ]Okinaka Memorial Institute for Medical Research , Toranomon Hospital, Tokyo, Japan
                [3 ]Department of Pathology , Toranomon Hospital, Tokyo, Japan
                [4 ]Department of Pathology , Graduate School of Medicine, Yokohama City University, Yokohama, Japan
                Author notes
                Correspondence should be addressed to Y Oda or Y Ubara; Email: yasuhirooda3@ 123456gmail.com or ubara@ 123456toranomon.gr.jp
                Article
                EDM190092
                10.1530/EDM-19-0092
                6865358
                31743098
                8d1998cc-63d2-47c1-9ee4-52bc2eda91ea
                © 2019 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License..

                History
                : 16 September 2019
                : 03 October 2019
                Categories
                Adult
                Male
                Asian - Japanese
                Japan
                Kidney
                Diabetes
                Insulin
                Diabetes Mellitus Type 2
                Diabetic Foot Syndrome
                Diabetic Nephropathy
                Diabetes mellitus type 2
                Diabetic neuropathy
                Diabetic nephropathy
                Diabetic foot neuropathy
                Retinopathy
                Hypertension
                Polar vasculosis*
                Proteinuria
                Peripheral oedema
                Diabetic foot ulceration
                Leg pain
                Paraesthesia
                Neovascularization*
                Histopathology
                Estimated glomerular filtration rate
                Urinalysis
                Haemoglobin A1c
                Renal biopsy
                Angiography
                C-peptide (blood)
                Glucose (blood)
                Immunoglobulin A
                Insulin
                Creatinine (serum)
                Diet
                Clopidogrel
                Lansoprazole*
                Nifedipine
                Rosuvastatin*
                Aspirin
                Metformin
                Insulin glulisine
                Insulin degludec*
                Nephrology
                Unique/Unexpected Symptoms or Presentations of a Disease
                Unique/Unexpected Symptoms or Presentations of a Disease

                adult,male,asian - japanese,japan,kidney,diabetes,insulin,diabetes mellitus type 2,diabetic foot syndrome,diabetic nephropathy,diabetic neuropathy,diabetic foot neuropathy,retinopathy,hypertension,polar vasculosis*,proteinuria,peripheral oedema ,diabetic foot ulceration,leg pain,paraesthesia,neovascularization*,histopathology,estimated glomerular filtration rate,urinalysis,haemoglobin a1c,renal biopsy,angiography,c-peptide (blood),glucose (blood),immunoglobulin a,creatinine (serum),diet,clopidogrel,lansoprazole*,nifedipine,rosuvastatin*,aspirin,metformin,insulin glulisine,insulin degludec*,nephrology,unique/unexpected symptoms or presentations of a disease,november,2019

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